Evidence map›Paper›PMID 36143345›Full record

ArticleLife (Basel, Switzerland)2022

Characterization of a mGluR5 Knockout Rat Model with Hallmarks of Fragile X Syndrome.

Victoria Dahl, Hawley Helmbrecht, Ana Rios Sigler, Kate Hildahl, Holly Sullivan, Sanjana Janakiraman, Saahiti Jasti, Elizabeth Nance

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Unveiling the molecular mechanism of GProtein science : a publication of the Protein Society · 2025
    Article
  3. Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Victoria DahlDepartment of Chemical Engineering, University of Washington, Seattle, WA 98195, USA.ORCID 0000-0002-9632-9374
Hawley HelmbrechtDepartment of Chemical Engineering, University of Washington, Seattle, WA 98195, USA.ORCID 0000-0002-4797-0130
Ana Rios SiglerDepartment of Bioengineering, University of Washington, Seattle, WA 98105, USA.ORCID 0000-0002-5094-8073
Kate HildahlDepartment of Chemical Engineering, University of Washington, Seattle, WA 98195, USA.
Holly SullivanDepartment of Chemical Engineering, University of Washington, Seattle, WA 98195, USA.
Sanjana JanakiramanPaul Allen School of Computer Science and Engineering, University of Washington, Seattle, WA 98195, USA.
Saahiti JastiDepartment of Biology, University of Washington, Seattle, WA 98195, USA.
Elizabeth NanceDepartment of Chemical Engineering, University of Washington, Seattle, WA 98195, USA.ORCID 0000-0001-7167-7068
University of Washington · US

Funding

Burroughs Wellcome Fund Career Award at Scientific Interfaces
6 · The paper itself

Abstract

The number of reported cases of neurodevelopmental disorders has increased significantly in the last few decades, but the etiology of these diseases remains poorly understood. There is evidence of a fundamental link between genetic abnormalities and symptoms of autism spectrum disorders (ASDs), and the most common monogenetic inheritable form of ASDs is Fragile X Syndrome (FXS). Previous studies indicate that FXS is linked to glutamate signaling regulation by the G-protein-coupled metabotropic glutamate receptor 5 (mGluR5), which has been shown to have a regulatory role in neuroinflammation. We characterized the effect of knocking out mGluR5 in an organism known to have complex cognitive functions-the rat. The heterozygous phenotype is the most clinically relevant; therefore, we performed analysis in heterozygous pups. We showed developmental abnormalities in heterozygous mGluR5 knockout rats, as well as a significant increase in chemokine (C-X-C motif) ligand 1 (CXCL) expression, a hallmark indicator of early onset inflammation. We quantified an increase in microglial density in the knockout pups and quantified morphological phenotypes representative of greater reactivity in the male vs. female and postnatal day 28 heterozygous pups compared to postnatal day 14 heterozygous pups. In response to injury, reactive microglia release matrix metalloproteases, contribute to extracellular matrix (ECM) breakdown, and are responsible for eradicating cellular and molecular debris. In our study, the changes in microglial density and reactivity correlated with abnormalities in the mRNA expression levels of ECM proteins and with the density of perineuronal nets. We saw atypical neuropsychiatric behavior in open field and elevated plus tests in heterozygous pups compared to wild-type litter and age-matched controls. These results demonstrate the pathological potential of the mGluR5 knockout in rats and further support the presence of neuroinflammatory roots in ASDs.

Indexed as

autism spectrum disorders (ASDs)extracellular matrixmachine learningmicroglianeurodevelopmental disordersneuroinflammation

Identifiers

PMID36143345
PMCPMC9504063
OpenAlexW4293217670

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.